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    KCI등재 SCOPUS SCIE

    Sustainable degradation of carbon tetrafluoride to non-corrosive useful products by incorporating reduced electron mediator within electro-scrubbing

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    https://www.riss.kr/link?id=A106054353

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    다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

    The degradation of CF4 gas using existing technologies produces other types of greenhouse gas (CO2) and corrosive side products. The main aim of this study is to degrade CF4 gas at room temperature into useful products without producing corrosive side products by mediated electrochemical reduction (MER) process using an electrogenerated Cu1+[Ni2+(CN)4]1− mediator. Initial studies on the electrolytic reduction of the hetero-bimetallic complex in catholyte solution at anodized Ti cathode was monitored by oxidation/reduction potential (ORP) variation whether the Cu2+ or Ni2+ was reduced in the Cu2+[Ni2+(CN)4] and confirmed by electron spin resonance (ESR) spectroscopy the Cu1+[Ni2+(CN)4]1− formation. The concentration variation of Cu1+[Ni2+(CN)4]1− during CF4 injection demonstrated the degradation of CF4 followed the MER by electrogenerated Cu1+[Ni2+(CN)4]1−. Maximum removal efficiency of CF4 using electroscrubbing process was 96% at room temperature. Through the variation in gas phase parameters, the gas phase mass transfer coefficient was calculated that can facilitate scale up the developed process. Fourier transform infrared spectroscopy analysis in both the gas and solution phases showed that CH3CH2OH was the main product that formed during the removal of CF4 by electrogenerated Cu1+[Ni2+(CN)4]1− at electroscrubber along with a small amount of CF3CH3 intermediate. Importantly, this mechanism also avoided formation of the corrosive product HF.
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    The degradation of CF4 gas using existing technologies produces other types of greenhouse gas (CO2) and corrosive side products. The main aim of this study is to degrade CF4 gas at room temperature into useful products without producing corrosive side...

    The degradation of CF4 gas using existing technologies produces other types of greenhouse gas (CO2) and corrosive side products. The main aim of this study is to degrade CF4 gas at room temperature into useful products without producing corrosive side products by mediated electrochemical reduction (MER) process using an electrogenerated Cu1+[Ni2+(CN)4]1− mediator. Initial studies on the electrolytic reduction of the hetero-bimetallic complex in catholyte solution at anodized Ti cathode was monitored by oxidation/reduction potential (ORP) variation whether the Cu2+ or Ni2+ was reduced in the Cu2+[Ni2+(CN)4] and confirmed by electron spin resonance (ESR) spectroscopy the Cu1+[Ni2+(CN)4]1− formation. The concentration variation of Cu1+[Ni2+(CN)4]1− during CF4 injection demonstrated the degradation of CF4 followed the MER by electrogenerated Cu1+[Ni2+(CN)4]1−. Maximum removal efficiency of CF4 using electroscrubbing process was 96% at room temperature. Through the variation in gas phase parameters, the gas phase mass transfer coefficient was calculated that can facilitate scale up the developed process. Fourier transform infrared spectroscopy analysis in both the gas and solution phases showed that CH3CH2OH was the main product that formed during the removal of CF4 by electrogenerated Cu1+[Ni2+(CN)4]1− at electroscrubber along with a small amount of CF3CH3 intermediate. Importantly, this mechanism also avoided formation of the corrosive product HF.

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    참고문헌 (Reference)

    1 A.R. Ravishankara, 259 : 194-, 1993

    2 K.P. Kuhl, 5 : 7050-, 2012

    3 C. Rittmeyer, 26 : 2129-, 1993

    4 C.W. Lee, 116-117 : 455-, 1996

    5 H.M. Lee, 44 : 5526-, 2005

    6 A. Gal, 107 : 8859-, 2003

    7 X.-F. Xu, 266 : 131-, 2007

    8 M.S. Gandhi, 24 : 1234-, 2012

    9 Narengerile, 30 : 813-, 2010

    10 H. Zhang, 55 : 301-, 2005

    1 A.R. Ravishankara, 259 : 194-, 1993

    2 K.P. Kuhl, 5 : 7050-, 2012

    3 C. Rittmeyer, 26 : 2129-, 1993

    4 C.W. Lee, 116-117 : 455-, 1996

    5 H.M. Lee, 44 : 5526-, 2005

    6 A. Gal, 107 : 8859-, 2003

    7 X.-F. Xu, 266 : 131-, 2007

    8 M.S. Gandhi, 24 : 1234-, 2012

    9 Narengerile, 30 : 813-, 2010

    10 H. Zhang, 55 : 301-, 2005

    11 X. Xu, 20 : 543-, 2011

    12 Y. Takita, 1 : 4501-, 1999

    13 M.M. Farris, 11 : 501-, 1992

    14 N. Sonoyama, 32 : 375-, 1998

    15 P.L. Cabot, 151 : B98-, 2004

    16 E.R. Wagoner, 160 : G135-, 2013

    17 A. Schizodimou, 471 : 26-, 1999

    18 E.R. Wagoner, 676 : 6-, 2012

    19 P.L. Cabot, 6 : B15-, 2003

    20 R.E. Taylor-Smith, 99 (99): 116-, 1999

    21 G. Muthuraman, 325 : 157-, 2017

    22 Z.M. El-Bahy, 40 : 81-, 2003

    23 Y. Takita, 417-, 1999

    24 J.-Y. Song, 370 : 50-, 2013

    25 A.M. Chippindale, 44 : 12502-, 2015

    26 W.-T. Tsai, 15 : 65-, 2002

    27 M.G. Savelieff, 105 : 7919-, 2008

    28 P. Scharlin, 21 : 67-, 1992

    29 Y. Song, 1 : 6055-, 2016

    30 W.C. Fernelius, "Potassium tetracyanonickelate(II), Inorganic Syntheses" John Wiley & Sons Inc. 227-, 2007

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    학술지 이력
    연월일 이력구분 이력상세 등재구분
    2023 평가 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
    2020-01-01 등재 등재학술지 유지 (해외등재 학술지 평가) KCI등재
    2011-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2009-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2007-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2004-01-01 등재 등재학술지 선정 (등재후보2차) KCI등재
    2003-01-01 등재 등재후보 1차 PASS (등재후보1차) KCI등재후보
    2001-07-01 등재 등재후보학술지 선정 (신규평가) KCI등재후보
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    기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
    2016 3.4 0.75 2.84
    KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
    2.39 2.24 0.397 0.56
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